Hotchkiss A K, Parks-Saldutti L G, Ostby J S, Lambright C, Furr J, Vandenbergh J G, Gray L E
Deparment of Zoology, North Carolina State University, Raleigh, North Carolina 27695, USA.
Biol Reprod. 2004 Dec;71(6):1852-61. doi: 10.1095/biolreprod.104.031674. Epub 2004 Jul 30.
Prenatal exposure to environmental chemicals that interfere with the androgen signaling pathway can cause permanent adverse effects on reproductive development in male rats. The objectives of this study were to 1) determine whether a documented antiandrogen butyl benzyl phthalate (BBP) and/or linuron (an androgen receptor antagonist) would decrease fetal testosterone (T) production, 2) describe reproductive developmental effects of linuron and BBP in the male, 3) examine the potential cumulative effects of linuron and BBP, and 4) investigate whether treatment-induced changes to neonatal anogenital distance (AGD) and juvenile areola number were predictive of adult reproductive alterations. Pregnant rats were treated with either corn oil, 75 mg/kg/day of linuron, 500 mg/kg/day of BBP, or a combination of 75 mg/kg/day linuron and 500 mg/kg/day BBP from gestational Day 14 to 18. A cohort of fetuses was removed to assess male testicular T and progesterone production, testicular T concentrations, and whole-body T concentrations. Male offspring from the remaining litters were assessed for AGD and number of areolae and then examined for alterations as young adults. Prenatal exposure to either linuron or BBP or BBP + linuron decreased T production and caused alterations to androgen-organized tissues in a dose-additive manner. Furthermore, treatment-related changes to neonatal AGD and infant areolae significantly correlated with adult AGD, nipple retention, reproductive malformations, and reproductive organ and tissue weights. In general, consideration of the dose-response curves for the antiandrogenic effects suggests that these responses were dose additive rather than synergistic responses. Taken together, these data provide additional evidence of cumulative effects of antiandrogen mixtures on male reproductive development.
产前暴露于干扰雄激素信号通路的环境化学物质可对雄性大鼠的生殖发育造成永久性不良影响。本研究的目的是:1)确定已被记录的抗雄激素邻苯二甲酸丁苄酯(BBP)和/或利谷隆(一种雄激素受体拮抗剂)是否会降低胎儿睾酮(T)的生成;2)描述利谷隆和BBP对雄性生殖发育的影响;3)研究利谷隆和BBP的潜在累积效应;4)调查治疗引起的新生儿肛门生殖器距离(AGD)和幼年乳晕数量的变化是否可预测成年后的生殖改变。从妊娠第14天至18天,给怀孕大鼠分别灌胃玉米油、75毫克/千克/天的利谷隆、500毫克/千克/天的BBP,或75毫克/千克/天利谷隆与500毫克/千克/天BBP的混合物。取出一组胎儿以评估雄性睾丸T和孕酮的生成、睾丸T浓度以及全身T浓度。对其余窝中的雄性后代评估AGD和乳晕数量,然后在其成年后检查有无改变。产前暴露于利谷隆、BBP或BBP + 利谷隆均可降低T的生成,并以剂量相加的方式导致雄激素组织化的组织发生改变。此外,与治疗相关的新生儿AGD和婴儿乳晕变化与成年后的AGD、乳头保留、生殖畸形以及生殖器官和组织重量显著相关。总体而言,考虑到抗雄激素作用的剂量反应曲线,这些反应是剂量相加而非协同反应。综上所述,这些数据为抗雄激素混合物对雄性生殖发育的累积效应提供了更多证据。